A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5638980



Internal ID21587285
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:2662898..2662898hg38UCSC Ensembl
chr9:2662898..2662898hg19UCSC Ensembl
Cytoband9p24.2
Allele length
AssemblyAllele length
hg38178
hg19178
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17161465
SamplesNA19238
Known Genes
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nsv5638980
Frequency
Sample Size35
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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